PULLUP PULL900000
GUDID 03760304680786
Complete instrumentation set composed of reusable surgical instruments intended to be used for arthroscopic reconstruction of the ACL.
S.B.M
Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable| Primary Device ID | 03760304680786 |
| NIH Device Record Key | af2cd077-58af-462c-8cfa-660f5e182aef |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PULLUP |
| Version Model Number | PULLUP ligamentoplasty complete instrumentation se |
| Catalog Number | PULL900000 |
| Company DUNS | 772462123 |
| Company Name | S.B.M |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03760304680786 [Primary] |
FDA Product Code
| LXH | Orthopedic Manual Surgical Instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
[03760304680786]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-20 |
| Device Publish Date | 2024-06-12 |
On-Brand Devices [PULLUP]
| 03760154008976 | The Pullup® adjustable juxtacortical fixation device consists of an adjustable nonabsorbable br |
| 03760154008969 | The Pullup® adjustable juxtacortical fixation device consists of an adjustable nonabsorbable br |
| 03760154007122 | The Pullup® adjustable cortical fixation device consists of an adjustable nonabsorbable braided |
| 03760154007115 | The Pullup® adjustable cortical fixation device consists of an adjustable nonabsorbable braided |
| 03760154006163 | PULLUP® Ø 4.5 mm cannulated drill bit, to be used with PULLUP and BT LOOP adjustable fixation |
| 03760154006156 | PULLUP® Cutting pliers, to be used with PULLUP and BT LOOP adjustable fixation devices for ACL |
| 03760154003704 | The Reusable suture retriever pin is intended to be used with PULLUP and BT LOOP adjustable fixa |
| 03760304680786 | Complete instrumentation set composed of reusable surgical instruments intended to be used for a |
Trademark Results [PULLUP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PULLUP 87428871 not registered Live/Pending |
pullup Technologies Inc. 2017-04-27 |
 PULLUP 72194548 0813445 Dead/Expired |
AUTO GLASS MANUFACTURING CO. 1964-05-29 |
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